Ankle fusion device, instrumentation and methods

ABSTRACT

An ankle fusion device has a proximal portion generally aligned with a first longitudinal axis. The proximal portion includes a proximal end and a first fastener hole. The proximal portion has an arcuate curve such that the proximal end is spaced a distance from the first longitudinal axis in a first direction. The first fastener hole is configured to receive a first fastener along a first fastener axis. A distal portion of the ankle fusion device extends to a distal end from the proximal portion along a second longitudinal axis. The second longitudinal axis is angled in second and third directions relative to the first longitudinal axis. The second direction is perpendicular to the first direction and the third direction being opposite the first direction. The distal portion includes a second fastener hole configured to receive a second fastener along a second fastener axis.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 12/965,691 filed Dec. 10, 2010, which claims the benefit of U.S. Provisional Patent Application No. 61/284,141 filed Dec. 11, 2009 and entitled “Ankle Fusion Device and Method”, both of which are hereby incorporated by reference in their entirety.

BACKGROUND OF THE INVENTION

The present invention, according to some embodiments, includes an implantable device, instrumentation and methods for fusing ankle bones of a mammalian patient. More particularly, in some embodiments, the invention is directed to an arthrodesis nail and instrumentation and methods for implanting the same to fuse the tibia, talus, and calcaneus bones of an ankle of a human patient.

BRIEF SUMMARY OF THE INVENTION

In one embodiment there is an ankle fusion device that includes a proximal portion generally extending along a first longitudinal axis. The proximal portion includes a proximal end and a first fastener hole. The proximal portion has an arcuate curve such that the proximal end is spaced a distance from the first longitudinal axis in a first direction. The first fastener hole is configured to receive a first fastener along a first fastener axis. A distal portion of the ankle fusion device extends to a distal end from the proximal portion along a second longitudinal axis. The second longitudinal axis is angled in second and third directions relative to the first longitudinal axis. The second direction is perpendicular to the first direction and the third direction is opposite the first direction. The distal portion includes a second fastener hole configured to receive a second fastener along a second fastener axis. In one embodiment, the second fastener hole is elongate and the distal portion further includes a bore extending proximally from the distal end along the second longitudinal axis. The bore is at least partially threaded. The distal portion further includes an elongate third fastener hole configured to receive a third fastener along a third fastener axis.

In a further embodiment, the ankle fusion device comprises a compression screw configured to be received in the bore and translate therein along the second longitudinal axis. In on embodiment, the compression screw includes an engagement portion having a concave surface configured to contact the third fastener when the third fastener is received in the third fastener hole and a threaded portion attachable to the engagement portion and having external threads configured to engage the threads of the bore. In one embodiment, the bore does not extend through the entire distal portion.

In a further embodiment, the ankle fusion device further comprises an end cap set screw having a closed distal end and external screws configured to engage the threads of the bore. In one embodiment, the distal portion includes a third fastener hole configured to receive a third fastener along a third fastener axis. In one embodiment, the second fastener axis is oriented at an oblique angle relative to the third fastener axis. In one embodiment, the second fastener axis and the third fastener axis lie on planes that are parallel to one another. In one embodiment, the third fastener axis is configured to be substantially aligned with a longest dimension of a talus once the ankle fusion device is implanted. In one embodiment, the proximal portion further comprises a fourth fastener hole configured to receive a fourth fastener along a fourth fastener axis. In one embodiment, the fourth fastener axis and the first fastener axis are substantially parallel. In one embodiment, the fourth fastener hole is elongate.

In one embodiment, the distal end includes a truncated surface that is generally perpendicular to the first longitudinal axis and oriented at an oblique angle relative to the second longitudinal axis. In one embodiment, the second fastener axis is configured to be substantially aligned with a longest dimension of a calcaneus bone once the ankle fusion device is implanted. In one embodiment, once the ankle fusion device is implanted in a body the proximal portion extends into a tibia, the distal portion extends through a calcaneus, the first direction is in an anterior direction, the second direction is in a lateral direction and the third direction is in a posterior direction. In one embodiment, the entire proximal portion is arcuate in the first direction. In one embodiment, the proximal portion is least partially cannulated. In one embodiment, the proximal portion is substantially solid.

In another embodiment, a device for positioning at least one guidewire in a calcaneus bone and talus bone comprises a frame configured and dimensioned to at least partially surround the calcaneus bone and the talus bone. The frame includes a guidewire target configured and dimensioned to be inserted between the talus bone and a tibia bone proximate a talar dome of the talus bone and a first guidewire sleeve radially disposed about a first guidewire axis. The first guidewire axis is aligned with the guidewire target.

In a further embodiment, the device includes a second guidewire template attached to the frame and having a second guidewire sleeve radially disposed about a second guidewire axis. In one embodiment, the second guidewire template includes an alignment guide extending therefrom. In one embodiment, the second guidewire axis extends towards the guidewire target when the alignment guide is substantially aligned with a pre-selected anatomical feature. In one embodiment, the pre-selected anatomical feature is a second metatarsal bone. In one embodiment, the second guidewire axis is positioned at an oblique angle relative to the first guidewire axis when the alignment guide is substantially aligned with the pre-selected anatomical feature. In on embodiment, the second guidewire template is configured to rotate about the first guidewire axis. In one embodiment, the second guidewire template is slideable and rotatable relative to the first guidewire sleeve.

In a further embodiment, the device includes a tibial alignment guide engaged with the frame and configured to extend proximally therefrom along a longitudinal axis substantially parallel to the first guidewire axis. In one embodiment, the tibial alignment guide includes a transverse member being positionable at a location along a longitudinal axis of the tibial alignment guide. In one embodiment, the transverse member has a curvature about the first guidewire axis. In one embodiment, the frame further comprises a targeting arm that includes the guidewire target and the tibial member is attachable to the targeting arm. In one embodiment, an extension of the tibial alignment guide includes at least one alignment member, the at least one alignment member configured and positioned to intersect with a plane aligned with the first guidewire axis. In one embodiment, the tibial alignment guide is rotatably attachable with the frame.

In one embodiment, the frame further comprises a targeting arm that includes the guidewire target, the targeting arm and the first sleeve arm being substantially parallel to one another. In one embodiment, the first sleeve is fixed in position relative to the targeting arm. In one embodiment, the first guidewire axis is configured to substantially align with a center of the talar dome and to the guidewire target when the guidewire target is inserted between the talus and the tibia proximate the talar dome. In one embodiment, the first sleeve arm is positioned distally from the calcaneus bone when the guidewire target is inserted between the talus bone and the tibia bone proximate the talar dome of the talus bone.

In another embodiment, a method for positioning a guidewire in a calcaneus bone, talus bone, and tibia bone, includes: inserting a guidewire target on a guidewire targeting device into an ankle joint at a distal end of the tibia bone such that the guidewire target is proximate a talar dome of the talus bone; positioning a first guidewire sleeve on the guidewire targeting device proximate the calcaneus bone, the first guidewire sleeve pointing toward the guidewire target to provide a first guidewire axis; aligning the first guidewire axis of the first guidewire sleeve generally co-axially with a longitudinal axis of the tibia bone; and advancing a first guidewire along the first guidewire axis through the first guidewire sleeve and into the distal tibia bone through the calcaneus bone and talar dome of the talus bone.

In a further embodiment, the method includes: positioning a second guidewire axis of a guidewire template coupled to the guidewire targeting device at an oblique angle relative to the first guidewire axis; aligning the second guidewire axis with the talar dome of the talus bone and; and advancing a second guidewire along the second guidewire axis through a second guidewire sleeve on the guidewire temple and into the calcaneus bone and the talar bone until an end of the second guidewire generally reaches the first guidewire.

In one embodiment, the second guidewire axis includes rotating the guidewire template relative to the guidewire targeting device until an alignment arm of the guidewire template is substantially aligned with an anatomical feature. In one embodiment, the anatomical feature is a long axis of a second metatarsal bone. In one embodiment, the guidewire template is rotatably coupled to the guidewire targeting device. In one embodiment, the guidewire temple is slideably coupled over a portion of the first guidewire sleeve surrounding the first guidewire axis.

In a further embodiment, the method includes: removing the first guidewire; advancing a cannulated resection device over the second guidewire and through the calcaneus and the talus; performing a dorsiflexion and inversion of the ankle joint to align the second guidewire with the longitudinal axis of the tibia bone; advancing the second guidewire into the tibia bone along the longitudinal axis of the tibia bone; and further advancing the cannulated resection device over the second guidewire and into the tibia.

In one embodiment, the second guidewire axis is angled laterally and posteriorly relative to the first guidewire axis. In a further embodiment, the method comprises: positioning an elongate member coupled with the guidewire targeting device substantially parallel to the longitudinal axis of the tibia bone. In one embodiment, a proximal arm extends from the guidewire target and a distal arm extends from the first guidewire sleeve, the proximal arm being generally parallel to and spaced from the distal arm. In one embodiment, aligning the first guidewire axis includes aligning the guidewire target with a center of the talar dome.

In a further embodiment, the method includes bracing an alignment guide of the guidewire targeting device against an anterior surface of an outside of a leg. In one embodiment, aligning the first guidewire axis of the first guidewire sleeve generally co-axially with the longitudinal axis of the tibia bone includes positioning an alignment member of the guidewire targeting device proximal the tibia bone on a plane aligned with the longitudinal axis of the tibia bone.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

The foregoing summary, as well as the following detailed description of embodiments of the Ankle Fusion Device, Instrumentation and Methods, will be better understood when read in conjunction with the appended drawings of an exemplary embodiment. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.

In the drawings:

FIG. 1A is a posterior elevational view of an ankle fusion device including a nail in accordance with an exemplary embodiment of the present invention shown implanted in a semi-transparent skeleton;

FIG. 1B is a lateral elevational view of the nail shown in FIG. 1A;

FIG. 2A is a lateral elevational view of the nail of FIG. 1A;

FIG. 2B is an anterior elevational view of the nail of FIG. 1A;

FIG. 3 is a partial perspective view of a distal portion of the nail of FIG. 1A illustrating the use of a compression screw in accordance with an exemplary embodiment of the present invention;

FIG. 4 is an exploded perspective view of the compression screw of FIG. 3 and end caps for use with the ankle fusion device of FIG. 1A;

FIG. 5 is a posterior perspective view of a guidewire targeting device in accordance with an exemplary embodiment of the present invention;

FIG. 6 is a ventral or bottom plan view of a guidewire template in accordance with an exemplary embodiment of the present invention;

FIG. 7 is a perspective view of the guidewire targeting device of FIG. 5 in use with a guidewire template of FIG. 6 showing first and second guidewire axes;

FIG. 8A is a lateral elevational view of the guidewire targeting device of FIG. 5 in use upon initial insertion;

FIG. 8B is an anterior elevational view of the guidewire targeting device shown in FIG. 8A;

FIG. 8C is an enlarged lateral elevational view of the guidewire targeting device shown in FIG. 8A;

FIG. 9 is a dorsal or top plan view of a target on the talar dome of the talus;

FIG. 10 is a lateral elevational view of the guidewire targeting device shown in FIG. 8A in use with a first guidewire;

FIG. 11 is a ventral or bottom plan view of the guidewire targeting device and guidewire template of FIG. 7 in use with the first and second guidewires;

FIG. 12 is a lateral elevational view of the guidewire targeting device and guidewire template shown in FIG. 11;

FIG. 13 is a lateral elevational view of a cannulated drill being used with the second guidewire in accordance with an exemplary embodiment of the present invention;

FIG. 14 is a lateral elevational view of the second guidewire and cannulated drill of FIG. 13 and a protection sleeve in accordance with an exemplary embodiment of the present invention;

FIG. 15 is a lateral elevational view of a reamer being used in accordance with an exemplary embodiment of the present invention;

FIG. 16 is a lateral elevational view of a nail being inserted using an insertion handle in accordance with an exemplary embodiment of the present invention;

FIG. 17 is a medial elevational view of a calcaneus screw being inserted using an aiming arm in accordance with an exemplary embodiment of the present invention;

FIG. 18 is a medial elevational view of a talar screw being inserted using an aiming arm in accordance with an exemplary embodiment of the present invention;

FIG. 19 is a posterior elevational view of a first tibial screw being inserted using an aiming arm in accordance with an exemplary embodiment of the present invention;

FIG. 20 is an anterior elevational view of a second tibial screw being inserted using an aiming arm in accordance with an exemplary embodiment of the present invention;

FIG. 21 is a medial elevational view of a compression system of the ankle fusion device of FIG. 1;

FIG. 22 is a medial elevational view of end cap sleeve and end cap screw of FIG. 4 being inserted in the ankle fusion device of FIG. 1A;

FIG. 23A is a medial elevational view of the implanted ankle fusion device of FIG. 1A;

FIG. 23B is a lateral elevational view of the implanted ankle fusion device of FIG. 1A;

FIG. 23C is an anterior elevational view of the implanted ankle fusion device of FIG. 1A;

FIG. 23D is a posterior elevational view of the implanted ankle fusion device of FIG. 1A; and

FIG. 24 is a medial elevational view of the implanted nail of FIG. 1A attached to an extraction tool in accordance with an exemplary embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Referring to the drawings in detail, wherein like reference numerals indicate like elements throughout, there is shown in FIGS. 1A-24 an ankle fusion device, generally designated 10, and various instrumentation for implanting the same, in accordance with exemplary embodiments of the present invention.

Severe arthrosis and deformity of the ankle and subtalar joints may be debilitating problems that can be difficult to treat. Tibotalocalcaneal fusion (fusion of the calcaneus, talus and tibia) with an intramedullary nail can be considered a salvage procedure for severe arthrosis and deformity of the ankle and subtalar joints. Ankle arthrodesis may be a challenging procedure due to poor host conditions (e.g., bad skin, deformity, and avascular necrosis), inability to get adequate fixation for this slow healing process, and the inability to get adequate compression across the fusion. Performing an ankle arthrodesis can also be technically demanding because of the shape and small size of the talus and calcaneus. Furthermore, known methods of installing ankle arthrodeses may limit the optimal configuration of the nail and fixation screws.

Embodiments of ankle fusion device 10 are configured and shaped to obtain more optimal bony purchase in the calcaneus 12 and talus 14 and/or increase comfort. In some embodiments, ankle fusion device 10 obtains more optimal bony purchase and/or increase comfort by more accurately approximating the anatomy of the lower limb and using the instrumentation and methods described below to prepare the bones for implanting ankle fusion device 10. The embodiments disclosed below and shown in the drawings are for the left ankle. If not otherwise mentioned below, ankle fusion device 10, the instrumentation and methods are mirrored across the sagittal plane of the body for the right ankle.

Referring to FIGS. 1A and 1B, an exemplary ankle fusion device 10 is shown implanted within the calcaneus 12, talus 14 and tibia 16 of a patient. Ankle fusion device 10 includes a nail 18 and a plurality of fasteners 20. Fasteners 20 may include any fastening device such as but not limited to pegs, nails, wires, screws, fixation screws, bone screws and locking screws. In some embodiments, nail 18 is constructed from titanium, stainless steel, alloy, ceramic, and/or other solid biocompatible material. In some embodiments, nail 18 is substantially rigid. In some embodiments, at least a portion of an exterior surface of nail 18 is treated to improve biocompatibility and/or osteointegration (e.g., textured, titanium plasma spray coating, hydroxyapatite coating, etc.).

Referring to FIGS. 2A and 2B, an exemplary embodiment of nail 18 for the left ankle is shown. Nail 18 includes a proximal portion 18 a having an axis A₁ generally extending along, or in the direction of, a first longitudinal axis L₁ that corresponds to the general vertical center of tibia 16 (or in other words, proximal portion 18 a is generally perpendicular to a transverse plane of the patient). Proximal portion 18 a includes a proximal end 18 b and at least one fastener hole (e.g., fastener hole 222 c) for receiving a fastener 20. Nail 18 also includes a distal portion 18 c extending to a distal end 18 d from proximal portion 18 a along a second longitudinal axis L₂ co-axially aligned with axis A₂. Second longitudinal axis L₂ is oriented at an oblique angle relative to first longitudinal axis L₁. In one embodiment, nail 18 extends laterally and proximally downwardly or ventrally through the calcaneus once implanted.

In one embodiment, nail 18 also arcs anteriorly as it extends upwardly through the tibia 16 such that at least a portion of proximal portion 18 a is arcuate. In one embodiment, the entire proximal portion 18 a is arcuate. In one embodiment first longitudinal axis L₁ is tangent to the distal most end of axis A₁ of proximal portion 18 a. Having an arcuate proximal portion 18 a may help in positioning and/or fixing nail 18 within the canal of tibia 16. In one embodiment, proximal portion 18 a has an arcuate curve such that proximal end 18 b is spaced a distance d_(p) from first longitudinal axis L₁ in a first direction d₁. In one embodiment, distance d_(p) is about 36 mm for a 300 mm long nail 18. In one embodiment, proximal portion 18 a has a radius of curvature of about 1.5 m. In one embodiment, the radius of curvature of proximal portion 18 a is generally equal to the radius of curvature of an anterior tibial canal surface.

In one embodiment, proximal end 18 b is spaced a distance d_(p) from first longitudinal axis L₁ in a first direction d₁ and second longitudinal axis L₂ is oriented at oblique angles in second and third directions d₂, d₃ relative to first longitudinal axis L₁. In one embodiment, second direction d₂ is perpendicular to first direction d₁ and third direction d₃ is opposite first direction d₁. In one embodiment, once nail 18 is implanted, first direction d₁ corresponds to a forward or anterior direction, second direction d₂ corresponds to an outward or lateral direction and third direction d₃ corresponds to a rear or posterior direction relative to the ankle. In an alternative embodiment, proximal portion 18 a is substantially straight. In one such embodiment, proximal portion 18 a is co-axial with first longitudinal axis L₁.

In one embodiment, once ankle fusion device 10 is implanted in a body, proximal portion 18 a extends into tibia 16, distal portion 18 c extends through calcaneus 12, first direction d₁ is in an anterior direction, second direction d₂ is in a lateral direction and third direction d₃ is in a posterior direction. In some embodiments, proximal end 18 b is tapered or pointed, in order to facilitate insertion into the canal of tibia 16. In some embodiment, proximal end 18 b is tapered and configured to prevent a stress concentration on the canal of tibia 16 once nail 18 is implanted that may otherwise be caused by a nail end having a sharp edge. In one embodiment, proximal end 18 b is a blunt or rounded tip. In one embodiment, proximal end 18 b is closed.

In one embodiment, nail 18 has a generally circular cross section throughout its length. In alternative embodiments, nail 18 may have any cross section shape including but not limited to square, star, rectangular and triangular. In one embodiment, nail 18 has a plurality of sections that decrease in diameter toward a proximal end 18 b. In some embodiments, nail 18 tapers or decreases in cross sectional size between distal portion 18 c and proximal portion 18 a. In some embodiments, distal portion 18 c has a larger diameter than the largest diameter of proximal portion 18 a. In one embodiment, distal portion 18 c has a substantially constant diameter. In one embodiment, distal portion 18 c has a diameter of about 8 mm to about 18 mm. In one embodiment, distal portion 18 c has a diameter of about 13 mm.

In some embodiments, proximal portion 18 a includes a smaller diameter section and a larger diameter section. In one embodiment, the smaller diameter section is about 7 mm to about 11 mm. In one embodiment, the smaller diameter section is about 9 mm. In one embodiment, the larger diameter section is about 10 mm. In one embodiment, the larger diameter section is about 11.5 mm. In one embodiment, the larger diameter section is about 13 mm. In some embodiments, at least a portion of the larger diameter section is hollow. In some embodiments, the smaller diameter section is not hollow. In some embodiments, the smaller diameter section is proximal to the larger diameter section and distal to proximal end 18 b. In some embodiments, nail 18 is substantially solid. In some embodiments, nail 18 is hollow or cannulated.

In some embodiments, proximal portion 18 a includes a frustoconical section 18 h providing a transition between the larger diameter section and the smaller diameter section of the proximal portion 18 a. In some embodiments, frustoconical section 18 h is located at or proximate the center of the proximal portion 18 a (e.g., about midway along the length of proximal portion 18 a). In some embodiments, the smaller diameter section is shorter than the larger diameter section.

In other embodiments, the smaller diameter section is longer than the larger diameter section. in some embodiments, the smaller diameter section and the larger diameter section have lengths that are substantially equal. In some embodiments, nail 18 has a length of about 200 mm to about 300 mm.

In some embodiments, distal portion 18 c is configured to be positioned, at least partially, in talus and calcaneus bones 14, 12 of an ankle of the patient. In some embodiments, distal portion 18 c is oriented at an oblique angle relative to proximal portion 18 a to maximize purchase of distal portion 18 c in talus 14 and calcaneus 12 upon implantation of ankle fusion device 10. In some embodiments, distal portion 18 c is configured to be positioned in talus 14 and calcaneus 12 so as to generally pass through the center of talus 14 and calcaneus 12. In some embodiments, upon implantation, distal portion 18 c is angled posteriorly and/or laterally relative to proximal portion 18 a. In some embodiments, upon implantation, distal portion 18 c is angled posteriorly and/or laterally relative to a longitudinal axis of the tibia bone.

In the exemplary embodiment shown in FIGS. 2A and 2B, second longitudinal axis L₂ is oriented at an oblique angle relative to first longitudinal axis L₁ in third direction d₃ at an angle α of about 15 degrees as projected on to a coronal or x-y plane as shown in FIG. 2A. In the exemplary embodiment shown, second longitudinal axis L₂ is oriented at an oblique angle from first longitudinal axis L₁ in second direction d₂ at an angle β of about 10 degrees as projected on to a sagittal or y-z plane as shown in FIG. 2B. In an example for the embodiment shown, if nail 18 were removed, inverting the left foot 10 degrees and dorsiflexing the foot 15 degrees would co-axially align second longitudinal axis L₂ and first longitudinal axis L₁. In other embodiments, angle α may be about 5 degrees, about 6 degrees, about 7 degrees, about 8 degrees, about 9 degrees, about 10 degrees, about 11 degrees, about 12 degrees, about 13 degrees, about 14 degrees, exactly 15 degrees, about 16 degrees, about 17 degrees, about 18 degrees, about 19 degrees, about 20 degrees, about 21 degrees, about 22 degrees, about 23 degrees, about 24 degrees, about 25 degrees. In other embodiments, angle 0 may be about 1 degree, about 2 degrees, about 3 degrees, about 4 degrees, about 5 degrees, about 6 degrees, about 7 degrees, about 8 degrees, about 9 degrees, exactly 10 degrees, about 11 degrees, about 12 degrees, about 13 degrees, about 14 degrees, about 16 degrees, about 17 degrees, about 18 degrees, about 19 degrees, about 20 degrees.

Referring to FIGS. 1A and 1B, fastener holes 22 (e.g., 222 a, 222 b, 222 c, 222 d) extending through nail 18 are spaced along the length of nail 18 and are configured to receive fasteners 20. In some embodiments, ankle fusion device 10 includes a plurality of through holes or fastener holes 22, at least two of which being positioned at different locations along the length of nail 18, such that one of the at least two fastener holes 22 is positioned on nail 18 proximally or distally relative to the other fastener hole 22. In some embodiments, the ankle fusion device 10 includes a plurality of fastener holes 22, at least two of which are positioned at different radial locations about first and/or second longitudinal axes L₁, L₂ of nail 18. In some embodiments, one or more fastener holes 22 are positioned such that the central axes (see e.g., A₃-A₆) of each fastener hole 22 are substantially perpendicular to first and/or second longitudinal axis L₁, L₂ of nail 18. In some embodiments, one or more fastener holes 22 are oriented such that the central axes (e.g., A₃-A₆) through the one or more fastener holes 22 are not perpendicular to first and/or second longitudinal axis L₁, L₂ of nail 18. In some embodiments, ankle fusion device 10 includes a plurality of fastener holes 22, at least two of which are differently sized. In some embodiments, ankle fusion device 10 includes a plurality of fastener holes 22, at least two of which are substantially the same size. In some embodiments, at least some fastener holes 22 may have elongate openings, for example, elongated in a distal-proximal direction such that a fastener 20 positioned in such a fastener hole 22 is capable of shifting proximally or distally within the fastener hole 22. In some embodiments, at least some of fastener holes 22 (e.g, fastener hole 222 c may have substantially circular openings.

In one embodiment, a first fastener hole 222 a is configured to receive a first fastener 20 a for securing nail 18 to calcaneus 12 that is substantially co-axially aligned with a longest dimension of calcaneus 12 as shown. In one embodiment, first fastener hole 222 a is aligned with a central portion of calcaneus 12. For example, first fastener hole 222 a may be configured and oriented to have a central axis A₄ substantially co-axially aligned with a central longitudinal axis of calcaneus 12. Co-axial alignment of central axis A₄ with a central portion of the calcaneus bone allows first fastener 222 a, in some embodiments, to find greater purchase in calcaneus 12 and to permit a stronger securement thereto. In one embodiment, the central longitudinal axis of calcaneus 12 generally extends in an anterior direction. In some embodiments, first fastener 20 a has a length substantially matching the length of calcaneus 12 along a central longitudinal axis of calcaneus 12. In some embodiments, first fastener 20 a is about 70 mm to about 100 mm.

In one embodiment, a second fastener hole 222 b is configured to receive a second fastener 20 b for securing nail 18 to talus 14 that is substantially co-axially aligned with a longest dimension of talus 14 as shown. For example, second fastener hole 222 b may be configured (e.g., angled) to have a central axis A₃ substantially co-axially aligned with a central longitudinal axis of talus 14. In one embodiment, the central longitudinal axis of talus 14 generally extends in an anterior direction. In one embodiment, the central longitudinal axis of talus 14 generally extends in an anterior-medial direction. Co-axial alignment of the second fastener hole 222 b with a central portion of the talus bone allows the second fastener 20 b, in some embodiments, to find greater purchase in the talus 14 and to permit a stronger securement thereto. In one embodiment, the central longitudinal axis of talus 14 generally extends in an anterior-lateral direction. In some embodiments, second fastener 20 b has a length substantially matching the length of talus 14 along a central longitudinal axis of the talus 14. In some embodiments, second fastener 20 b is about 46 mm to about 80 mm.

Preferably, the central axes of the first and second elongate fastener holes 222 a, 222 b are divergent (e.g., as they extend anteriorly), such that the central axes are not parallel and/or not coplanar. Furthermore, the first elongate fastener hole 222 a may have a different (e.g., larger) dimension than the second elongate fastener hole 222 b, for example, so as to accept larger fasteners and/or permit greater shifting of the fastener.

Referring to FIGS. 2A and 2B, in one embodiment, first fastener hole 222 a is elongated such that first fastener 20 a can be translated proximally with respect to second longitudinal axis L₂ while being parallel with axis A₄. In one embodiment, axis A₄ is about 25 degrees to about 35 degrees relative to second longitudinal axis L₂. In one embodiment, axis A₄ is about 30 degrees relative to second longitudinal axis L₂. In one embodiment, second fastener hole 222 b is elongated such that second fastener 20 b can be translated with respect to second longitudinal axis L₂ while being parallel with axis A₃. In one embodiment, axis A₃ is about 85 degrees to about 95 degrees relative to second longitudinal axis L₂. In one embodiment, axis A₃ is generally perpendicular to second longitudinal axis L₂. In alternative embodiments, first and second fastener holes 222 a, 222 b are not elongated such that the respective fastener 20 a, 20 b generally cannot translate relative to nail 18.

Proximal portion 18 a includes at least one fastener hole 22. In one embodiment, proximal portion 18 a of nail 18 includes a locking or static fastener hole 222 c. In such an embodiment, the locking fastener hole 222 c is configured to receive a third fastener 20 c and sized to substantially prevent translational movement of third fastener 20 c relative to nail 18. In one embodiment, proximal portion 18 a of nail 18 includes a dynamic fastener hole 222 d. In one embodiment, dynamic fastener hole 222 d is elongated such that nail 18 can be translated proximally with respect to a fourth fastener 20 d extending through dynamic fastener hole 222 d. In such an embodiment and as described in further detail below, fourth fastener 20 d is installed toward the proximal end of dynamic fastener hole 222 d such that nail 18 is substantially prevented from moving distally with respect to tibia 16 but allows for a predetermined amount of proximal movement to allow for, for example, additional compression of the ankle joint. Either one of or both third fastener 20 c and fourth fastener 20 d may be used depending on whether it is desired to fix nail 18 relative to tibia 16.

In one embodiment, dynamic fastener hole 222 d has an axis A₅ such that fourth fastener 20 d can be translated distally with respect to first longitudinal axis L₁ while being parallel with axis A₅. In one embodiment, axis A₅ is substantially perpendicular to first longitudinal axis L₁ in the coronal or x-y plane as shown in FIG. 2B. In one embodiment, locking fastener hole 222 c has an axis A₆ that is substantially aligned with third fastener 20 c. In one embodiment, axis A₆ is substantially perpendicular to first longitudinal axis L₁ in the coronal or x-y plane as shown in FIG. 2B. In one embodiment, axes A₅ and A₆ are substantially parallel to one another. In alternative embodiments, axes A₅ and A₆ may be oriented at oblique angles with respect to first longitudinal axis L₁ and/or each other.

Referring to FIGS. 3 and 4, in embodiments with elongated fasteners holes 222 a and/or 222 b, nail 18 may include a compression mechanism to move two or more of calcaneus 12, talus 14 and tibia 16 closer together. To facilitate compression, in one embodiment, nail 18 includes a bore 18 e extending proximally from distal end 18 d along second longitudinal axis L₂. In one embodiment, bore 18 e is at least partially threaded. Ankle fusion device 10 may include a compression screw 324. In one embodiment, compression screw 324 is configured to be received in bore 18 e and translate therein along second longitudinal axis L₂. In one embodiment, compression screw 324 includes an engagement portion 324 a having a concave surface configured to contact first fastener 20 a when first fastener 20 a is received in first fastener hole 222 a. In one embodiment, engagement portion 324 a includes a projection 324 b extending into a groove 18 f in the bore 18 e to prevent the engagement portion 324 a from rotating about the second longitudinal axis L₂ as the engagement portion 324 a translates proximally up bore 18 e. In an alternative embodiment, bore 18 e includes a projection that is received in a corresponding groove in engagement portion 324 a.

The compression screw 324 includes a threaded portion 324 c attachable to engagement portion 324 a. Threaded portion 324 c includes threads configured to engage the threads of bore 18 e. In one embodiment, threaded portion 324 c is rotatably attached to engagement portion 324 a. In one embodiment, threaded portion 324 c includes an engagement member 324 d such as, for example a hexagon socket or slot, for mating with a screw driver tool 326. As threaded portion 324 c is rotated, compression screw 324 advances proximally through bore 18 e and translates first fastener 20 c proximally (e.g., across first fastener hole 222 a). Since first fastener 20 a is fixed relative to calcaneus 12 and at least one of third and fourth fasteners 20 c, 20 d keep nail 18 from being pulled distally, advancing compression screw 324 moves calcaneus 12 proximally toward talus 14.

Similarly, if second fastener hole 222 b is elongate, advancing compression screw 324 proximally moves talus 14 toward tibia 16. If both first and second fastener holes 222 a, 222 b are elongate, advancing compression screw 324 proximally moves both calcaneus and talus toward tibia 16 and compresses all three bones together. In one embodiment, bore 18 e extends entirely through distal portion 18 c. In one embodiment, bore 18 e extends substantially through the entire nail 18 such that nail 18 is generally hollow. In some embodiments, bore 18 e extends at least partially through distal portion 18 c. In an alternative embodiment, bore 18 e extends only through distal portion 18 c that is distal to first fastener hole 222 a.

Referring to FIGS. 3 and 4, ankle fusion device 10, includes, in one embodiment, an end cap screw 428 for closing bore 18 e after implantation and compression. In one embodiment, end cap screw 428 is threaded for engagement of the threads in bore 18 e. In an alternative embodiment, end cap screw 428 is not threaded and instead snap fits into bore 18 e.

In some embodiments, distal end 18 d of nail 18 includes a groove or step 18 g for engaging and orienting tools about and relative to second longitudinal axis L₂ as described in further detail below. In such embodiments, ankle fusion device 10 may include an end cap sleeve 430. End cap sleeve 430 includes one or more projections 430 a on a proximal end that are configured to align with groove 18 g and an end surface 430 b on a distal end that forms the distal most end of ankle fusion device 10. In one embodiment, end surface 430 b is configured to be substantially flush with the surrounding calcaneus 12 and with the end cap screw 428, proximate the end of bore 18 e.

In some embodiments, in order to insert nail 18 into the calcaneus 12, talus 14 and tibia 16, a path is created, e.g., by advancing (e.g., drilling) a hole proximally starting from the bottom of calcaneus 12. Referring to FIGS. 5-12, in some embodiments, one or more guidewires are inserted through the calcaneus 12, talus 14 and tibia 16 to fix reference axes for forming a path for nail 18.

Referring to FIG. 5, in some embodiments, a guidewire targeting device 534 is used in implanting ankle fusion device 10. The guidewire targeting device 534 may eliminate the need for less accurate freehand guidewire insertion techniques that are typically used to install an ankle arthrodesis. Guidewire targeting device 534 may use the orientation of the patient's anatomy (e.g., tibia 16, talus 14 and/or foot) to position at least one cutting apparatus (e.g., guidewire 1060) up through calcaneus 12, talus 14 and tibia 16 (see FIG. 10). In one embodiment, guidewire targeting device 534 is configured to account for the posterolateral bend of nail 18 as described above and sets the proper orientation for the drilling and placement of nail 18.

In one embodiment, guidewire targeting device 534 includes a frame 536 for at least partially surrounding the calcaneus 12 and talus 14. In one embodiment, frame 536 includes a target arm 538 having a guidewire target 538 a configured and dimensioned to be inserted between talus 12 and tibia 16 proximate a talar dome 14 a (see FIGS. 8c and 9) of talus 14. In one embodiment, first sleeve arm 540 is positioned distally from calcaneus 12 when the guidewire target 538 a is inserted between talus 14 and tibia 16 proximate talar dome 14 a. In one embodiment, guidewire target 538 a is a semi-circular indentation in the distal end of target arm 538. In alternative embodiments, guidewire target 538 a includes a marker that is visible using an imaging device such as but not limited to a radio-marker that is visible using an imaging device and/or a guide such as a slot, a hole or a projection. In one embodiment, target arm 538 includes one or more downwardly extending projections 538 b used to aid in aligning guidewire target 538 a with a center or apex 14 b of talar dome 14 a. In one embodiment, projections 538 b include a pair of projections 538 b positioned on either side of guidewire target 538 a. In one embodiment, the distal end of target arm 538 is thinner than the remainder of the frame 536 such that target arm 538 fits more easily between talus 14 and tibia 16 while maintaining the strength of the remainder of frame 536.

In order to align a first guidewire axis A₇ with the guidewire target 538 a, in one embodiment, frame 536 includes a first sleeve arm 540. In one embodiment, first sleeve arm 540 includes a proximal side facing towards target arm 538 and a distal side opposite the proximal side. In one embodiment, frame 536 is substantially C-shaped. In one embodiment, frame 536 is bent or at least arcuate such that target arm 538 extends above talar dome 14 a while first sleeve arm 540 extends under calcaneus 12. In one embodiment, target arm 538 and first sleeve arm 540 are substantially parallel. In one embodiment, first sleeve arm 540 includes a first guidewire sleeve 542. In one embodiment, first guidewire sleeve 542 is integral with first sleeve arm 540. In one embodiment, first guidewire sleeve 542 is detachable from first sleeve arm 540. In one embodiment, first guidewire sleeve 542 is positioned at or proximate a free end of first sleeve arm 540. In one embodiment, at least a portion of first guidewire sleeve 542 extends from the proximal side of first sleeve arm 540. In one embodiment, at least a portion of first guidewire sleeve 542 extends from the distal side of first sleeve arm 540. In one embodiment, first guidewire sleeve 542 extends from the proximal side and the distal side of first sleeve arm 540. In one embodiment, first guidewire sleeve 542 is fixed in position relative to guidewire target 538 a. In one embodiment, a central longitudinal axis of first guidewire sleeve 542 is configured to co-axially align with first guidewire axis A₇. In one embodiment, first guidewire sleeve 542 is fixed in position relative to target arm 538. In one embodiment, first guidewire sleeve 542 is radially disposed about first guidewire axis A₇. In one embodiment, first guidewire axis A₇ is aligned with guidewire target 538 a.

In order to co-axially align first guidewire axis A₇ with first longitudinal axis L₁, guidewire targeting device 534 may be aligned with and/or attached to at least one anatomical feature of the patient. In one embodiment, the at least one anatomical feature is tibia 16. In one embodiment, guidewire targeting device 534 includes a tibial member or alignment guide 544. In one embodiment, tibial alignment guide 544 is engaged with frame 536 and is configured to extend proximally therefrom along a longitudinal axis substantially parallel to the first guidewire axis A₇. In one embodiment, tibial alignment guide 544 is attached to target arm 538. In one embodiment, tibial alignment guide 544 is moveably attached to frame 536 using a fastener 544 b. In one embodiment, tibial alignment guide 544 is moveably attached to frame 536 using a star grind fastener such that tibial alignment guide 544 may be positioned relative to tibia 16 and frame 536 may be independently rotated about first longitudinal axis L₁ and then locked in position relative to tibial alignment guide 544 once in the appropriate position. In one embodiment, the position of frame 536 relative to tibial alignment guide 544 is adjustable but generally set by the surgeon prior to attaching to the patient. In one embodiment, the position of frame 536 relative to tibial alignment guide 544 is adjustable once guidewire targeting device 534 has been attached to the patient. In one embodiment, the position of frame 536 relative to tibial alignment guide 544 is radially adjustable. In alternative embodiments, transverse member 546 is fixed to frame 536.

To further aid in positioning guidewire targeting device 534, tibial alignment guide 544 may include a transverse member 546. In some embodiments, transverse member 546 extends generally perpendicularly from tibial alignment guide 544. In one embodiment, transverse member 546 is configured to have a curvature about first guidewire axis A₇, such that the transverse member 546 wraps at least partially around the leg during use. In one embodiment, the transverse member 546 is positionable at different locations along a length of tibial alignment guide 544 to aid in aligning first guide wire axis A₇ with first longitudinal axis L₁ during use as described further below. In one embodiment, tibial alignment guide 544 includes a longitudinal slot 544 a extending at least partially along a length of tibial alignment guide 544. In one embodiment, transverse member 546 includes a fastener 546 a such as a screw knob that extends through longitudinal slot 544 a. In alternative embodiments, transverse member 546 may be movable attached to or fixedly attached but moveable relative to tibial alignment guide 544 in any manner. In one embodiment, instead of a longitudinal slot 544 a, tibial alignment guide 544 includes a plurality of holes. In an alternative embodiment, transverse member 546 is fixed relative to or integral with tibial alignment guide 544.

In one embodiment, transverse member 546 is bendable or conformable such that the surgeon can shape transverse member 546 to the shape of the patient's leg. In one embodiment, transverse member 546 includes an attachment member (not shown) such as, for example, a Velcro strap and/or elastic band that is configured to attached to the patient's leg. In one embodiment, frame 536 and/or transverse member 546 may be attached to tibial alignment guide 544 in the opposite facing direction for use with the right ankle.

In one embodiment, frame 536 and/or tibial alignment guide 544 includes indicia (not shown) to indicate the proper orientation of or connection between components of guidewire targeting device 534 for the left and right foot. In one embodiment, frame 536 and/or transverse member 546 includes indicia (not shown) to indicate the general position frame 536 should be oriented to tibial alignment guide 544 depending on the position of the patient during surgery. In one embodiment, transverse member 545 includes indicia 546 b, 546 c to indicate the proper orientation for the left and right foot. In the embodiment illustrated, transverse member 546 is shaped for use when the patient is in the supine position. In some embodiments, a differently shaped transverse member 546 may be provided for patients in the prone position. In alternative embodiments, a single transverse member 546 is provided and frame 536 may be attached to tibial alignment guide 544 in a radial orientation relative to tibial alignment guide 544 depending on the position of the patient.

In one embodiment, transverse member 546 includes a first alignment member 546 d for aligning with the first longitudinal axis L₁ and/or first guidewire 1060 as described further below. In one embodiment, transverse member 546 includes a second alignment member 546 e for aligning with first longitudinal axis L₁ and/or first guidewire 1060. In one embodiment, first and/or second alignment members 546 d, 546 e are configured and positioned to intersect with a plane aligned with the first guidewire axis A₇. In one embodiment, first and second alignment members 546 d, 546 e include indents or bends in the transverse member 546. In one embodiment, first and second alignment members 546 d, 546 e include one or more projections and/or grooves in the transverse member 546. In alternative embodiments, first and second alignment members 546 d, 546 e include a marker that is visible using an imaging device such as but not limited to a radio-marker that is visible using an imaging device. In some embodiments, the horizontal thickness of first and second alignment members 546 d, 546 e is generally equal to a thickness of first guidewire 1060. In one embodiment, first alignment member 546 d is positioned along the length of transverse member 546 such that first alignment member 546 d aligns with first longitudinal axis L₁ from a lateral view of tibia 16 and second alignment member 546 e is positioned along the length of transverse member 546 e such that second alignment member 546 e aligns with first longitudinal axis L₁ from an anterior view of tibia 16. In one embodiment, aligning first and second alignment member 546 e with first longitudinal axis L₁ from two directions helps to ensure that tibial alignment guide 534 is substantially parallel with first longitudinal axis L₁.

Referring to FIGS. 6 and 7, guidewire targeting device 534 may include a second guidewire template 648 for use with a second guidewire 1262. Second guidewire template 648 is configured to align a second guidewire axis A₈ with the guidewire target 538 a. Second guidewire template 648 includes a second position sleeve 648 a radially disposed about a second guidewire axis A₈. In one embodiment, first guidewire sleeve 542 is used to co-axially align first guidewire axis A₇ with first longitudinal axis L₁ and second position sleeve 648 a is used to co-axially align second guidewire axis A₈ with the desired position of second longitudinal axis L₂. In one embodiment, guidewire targeting device 534 is configured to position second longitudinal axis L₁. In one embodiment, guidewire targeting device 534 is configured to align first longitudinal axis L₁ with the central longitudinal axis of tibia 16 and guidewire targeting device 534 is configured to position second longitudinal axis L₂ in a preselected orientation with respect to the position of first longitudinal axis L₁. In one embodiment, the preselected orientation is based on the shape of nail 18.

Second guidewire template 648 (see, e.g., FIG. 6) may be integral, moveable and/or detachable with frame 536. In one embodiment, second guidewire template 648 is removably attached to first sleeve arm 540. In one embodiment, second guidewire template 648 is positioned distally with respect to frame 536. In one embodiment, second guidewire template 648 is configured to abut the distal side of first sleeve arm 540. In one embodiment, second guidewire template 648 is positioned such that at least a portion of first sleeve arm 540 is located between second guidewire template 648 and target arm 538. In other embodiments, at least a portion of second guidewire template 648 is positioned between target arm 538 and first sleeve arm 540. In one embodiment, second guidewire template 648 includes an attachment sleeve 648 c. In one embodiment, attachment sleeve 648 c is configured and dimensioned to engage with at least a portion of first guidewire sleeve 542. In one embodiment, attachment sleeve 648 c is configured to engage with a portion of first guidewire sleeve 542 that extends from the distal side of first sleeve arm 540. In one embodiment, attachment sleeve 648 c is compression fit over first guidewire sleeve 542 such that attachment sleeve 648 c is moveable with respect to first guidewire sleeve 542 but remains in place relative to first guidewire sleeve 542 after first guidewire sleeve 542 is positioned and released by the surgeon. In one embodiment, attachment sleeve 648 c snap fits onto first guidewire sleeve 542 such that movement of attachment sleeve 648 c is retained along first guidewire axis A₇ but is free to rotate about first guidewire axis A₇. In one embodiment, second position sleeve 648 a is configured to rotate about first guidewire axis A₇. In one embodiment, second position sleeve 648 a is translatable along an arc about first guidewire axis A₇.

In one embodiment, second position sleeve 648 a is configured to be a retainer for receiving and aligning a second guidewire sleeve 1252 (see, e.g., FIG. 12) along second guidewire axis A₈. In an alternative embodiment, second guidewire sleeve 1252 is integral with second position sleeve 648 a.

Second guidewire template 648 may include an alignment arm 648 b for positioning second guidewire axis A₈ relative to first longitudinal axis L₁ by aligning alignment arm 648 b relative to an anatomical feature of the patient. In embodiments where second guidewire template 648 is moveable with respect to frame 536, alignment arm 648 b may be used to position second guidewire axis A₈ relative to first guidewire axis A₇ and relative to first longitudinal axis L₁ by aligning alignment arm 648 b relative to an anatomical feature of the patient. In one embodiment, second guidewire template 648 is configured such that second guidewire axis A₈ is substantially aligned with guidewire target 538 a and/or center 14 b of talar dome 14 a when alignment arm 648 b is aligned with a pre-selected anatomical feature of the patient. In one embodiment, alignment arm 648 b extends generally perpendicularly from first guidewire axis A₇. In one embodiment, the pre-selected anatomical feature aligned with the alignment arm 648 b is generally perpendicular to the central axis of tibia 16 (i.e., first longitudinal axis L₁). In one embodiment, the pre-selected anatomical feature is a second metatarsal bone 1150 (see FIG. 11). In one embodiment, alignment arm 648 b is aligned to be substantially parallel with second metatarsal 1150 to determine the position of second guidewire axis A₈. In alternative embodiments, the pre-selected anatomical feature is any one of the elongated bones in the foot.

Referring to FIGS. 8A-8B, in an exemplary embodiment in use, guidewire targeting device 534 is used to prepare the ankle for insertion of ankle fusion device 10. First and second guidewires 1060, 1262 may be used to properly align nail 18 with the patient's anatomy. In one embodiment, first guidewire 1060 is generally aligned with first longitudinal axis L₁ (e.g., the central longitudinal axis of tibia 16) and second guidewire 1262 is generally aligned with the position of second longitudinal axis L₂ once nail 18 is implanted (e.g., at an oblique angle relative to first longitudinal axis L₁). In one embodiment, first and second guidewires 1060, 1262 are used in order to form a cutting path corresponding to the bent shape of nail 18 using two generally straight lines. In alternative embodiments, a single guidewire may be used if the guidewire bends during insertion or if the foot is positioned such that the paths for the first and second longitudinal axes L₁, L₂ are co-axially aligned during insertion of the guidewire. In one embodiment, the use of first and second guidewires 1060, 1262 allows for more accurate alignment with first and second longitudinal axes L₁, L₂ since first guidewire 1060 is used to co-axially align with first longitudinal axis L₁ using anatomical features such as the talar dome 14 a and the tibia 16 and the second wire 1262 can be positioned relative to the first guidewire 1062 (or the path created by the first guidewire).

Before beginning the procedure, the position of the patient may be determined based on the type of arthrodesis procedure performed and the discretion of the surgeon. In one embodiment, the patient is placed in the prone position. In another embodiment, the patient is placed in the supine position. In some embodiments, for example, with a patient in the prone position, guidewire targeting device 534 is placed in the posterior (not shown) or posterolateral position (the position shown in the exemplary embodiment of FIGS. 8A-12). In alternative embodiments, for example, where a patient is in the supine position, the guidewire targeting device 534 may be placed in the anterolateral position.

Referring to FIGS. 8A-8C and 9, the foot may be oriented relative to tibia 16 in the position that the ankle is to be fixed in place. In one embodiment, the ankle is placed in a neutral position. In other embodiments, the ankle is placed in about 2 to about 3 degrees dorsi flexion. Once the ankle is in the desired position, guidewire target 538 a is inserted between talus 14 and tibia 16. In one embodiment, guidewire target 538 a is placed proximate talar dome 14 a (see FIG. 9). In one embodiment, guidewire target 538 a is placed proximate center 14 b of talar dome 14 a. In one embodiment, guidewire target 538 a is positioned generally directly above center 14 b of talar dome 14 a. In one embodiment, center 14 b of talar dome 14 a is aligned with first longitudinal axis L₁ and the central axis of tibia 16. In one embodiment, projections 538 b are positioned on either side of center 14 b of talar dome 14 a. In one embodiment, the position of guidewire target 538 a relative to talus 14 is viewed using imaging such as fluoroscopic imaging.

In addition to positioning guidewire target 538 a relative to talus 14, first guidewire sleeve 542 is positioned under calcaneus such that first guidewire axis A₇ generally aligns with guidewire target 538 a. In one embodiment, first guidewire sleeve 542 is positioned so that first guidewire sleeve 542 aligns exactly with guidewire target 538 a. In one embodiment, first guidewire sleeve 542 is positioned so that first guidewire axis A₇ is aligned with center 14 b of talar dome 14 a.

In one embodiment, tibial alignment guide 544 is used to help align the first guidewire axis A₇ with first longitudinal axis L₁ by positioning tibial alignment guide 544 substantially parallel with tibia 16. In one embodiment, first alignment member 546 d and/or second alignment member 546 e are aligned with first longitudinal axis L₁ in the lateral and anterior views, respectively, to position tibial alignment guide 544 substantially parallel with tibia 16.

In one embodiment, tibial alignment guide 544 is positioned relative to first longitudinal axis L₁ by sliding or otherwise positioning transverse member 546 along the length of tibial alignment guide 544 and in contact with the outer surface of the leg. In one embodiment, transverse member 546 prevents guidewire targeting device 534 from moving with respect to the patient. In one embodiment, without transverse member 546, guidewire targeting device 534 would pivot laterally and posteriorly relative to guidewire target 538 a caused by the weight of guidewire targeting device 534. In one embodiment, transverse member 546 counters any pivot of guidewire targeting device 534 with respect to the guidewire target 538 a. Due to the shape of the leg, in one embodiment, moving transverse member 546 along the length of tibial alignment guide 544 alters the orientation of first guidewire axis A₇ in a first plane until first guidewire axis A₇ is aligned with first longitudinal axis L₁. In one embodiment, the curvature of transverse member 546 keeps first guidewire axis A₇ aligned with first longitudinal axis L₁ in a second plane, the second plane being generally perpendicular to the first plane.

Referring to FIG. 10, once first guidewire axis A₇ is in the desired position, a first guidewire 1060 is advanced proximally through first guidewire sleeve 542, along first guide wire axis A₇, through calcaneus 12 and talus 14 and into the distal end of tibia 16. In one embodiment, the placement and guidance of first guidewire 1060 is monitored using the imaging device. In one embodiment, the guidance of first guidewire 1060 is monitored using the imaging device from lateral and mortise views. In one embodiment, first guidewire 1060 is aligned with first alignment member 546 d and/or second alignment member 546 e in the lateral and anterior views, respectively. Advancement of the first guidewire 1060 along first guidewire axis A₇, in some embodiments, creates a channel in the distal end of tibia 16 substantially aligned with first longitudinal axis L₁.

Referring to FIG. 11, if second guidewire template 648 is not already coupled with frame 536, second guidewire template 648 is attached to guidewire targeting device 534. In one embodiment, second guidewire template 648 include indicia 648 d (see FIG. 6) such as the word “Left” and/or color coding to indicate the appropriate left or right foot. Once the second guidewire template 648 is attached to guidewire targeting device 534, second guidewire template 648 may be positioned relative to frame 536 and/or first guidewire axis A₇ by aligning alignment arm 648 b with an anatomical feature of the patient such as second metatarsal 1150. Once second guidewire template 648 is in place second guidewire axis A₈ generally aligns with guidewire target 538 a and is co-axial with where second longitudinal axis L₂ will be. In one embodiment, once second guidewire template 648 is in place, second guidewire axis A₈ generally aligns with the anterior margin of the plantar aspect of the calcaneal tuberosity equidistant from the medial and lateral wall of calcaneus 12.

Referring to FIG. 12, in one embodiment, second guidewire sleeve 1252 is inserted into second position sleeve 648 a if second guidewire sleeve 1252 is not already attached. In one embodiment, second guidewire 1262 is advanced proximally through second guidewire sleeve 1252, through calcaneus 12 and talus 14 proximate the guidewire target 538 a. In one embodiment, the position of second guidewire 1060 during insertion is monitored using the imaging device from lateral and mortise views.

Referring to FIG. 13, in one embodiment, once second guidewire 1262 is in position, first guidewire 1062 and guidewire targeting device 534 are removed such that only second guidewire 1262 remains. In one embodiment, a cannulated drill 1356 is inserted over the second guidewire 1262. In alternative embodiments, the guidewire targeting device 534 is left in place, the second guidewire 1262 is removed and a drill is guided along second guidewire axis A₈.

Referring to FIG. 14, in one embodiment, once the cannulated drill 1356 has been advanced proximate the talar dome 14 a, the foot is positioned such that second guidewire 1262 aligns with first longitudinal axis L₁. In some embodiments, the foot is positioned such that second guidewire 1262 is substantially aligned with a longitudinal axis of tibia 16. In some embodiments, positioning the foot includes angling the foot relative to tibia 16 such that second guidewire 1262 is substantially aligned with the channel created in the distal end of tibia 16 by the first guidewire 1060. In some embodiments, second guidewire 1262 is then advanced into the channel created in the distal end of tibia 16 by the first guidewire 1060. In one embodiment, a protection sleeve 1458 is inserted over second guidewire 1262 to aid in positioning the foot and protects the cannulated drill 1356. In one embodiment, the foot is dorsiflexed about 15 degrees and inverted 10 degrees. In one embodiment, once the foot has been repositioned, cannulated drill 1356 is advanced into tibia 16 over second guidewire 1262.

Referring to FIG. 15, in one embodiment, once the cannulated drill 1356 and second guidewire 1262 are removed, it may be desirable to ream the canal of tibia 16. In one embodiment, a reamer 1564 is inserted through the path created by the cannulated drill 1356. A narrow tibial canal may hinder insertion of nail 18. In one embodiment, progressive reaming of the tibial canal is performed using reamers having cross sectional widths of about 0.5 mm to about 1 mm larger than the diameter of nail 18.

Referring to FIG. 16, once the pathway has been drilled, nail 18 may be inserted proximally through calcaneus 12 and talus 14 and into tibia 16. In one embodiment, an insertion handle 1666 is attached to distal end 18 d of nail 18 to aid in insertion of nail 18. Insertion handle 1666 is configured to align with the at least one groove 18 g in nail 18 so that the radial position of insertion handle 1666 is fixed relative to distal portion 18 c of nail 18. In one embodiment, insertion handle 1666 is coupled to distal portion 18 c of nail 18 using a threaded connecting screw (not shown) that extends upwardly into bore 18 e of nail 18. In one embodiment, nail 18 is inserted as far as possible by gripping the insertion handle and pushing nail 18 upwardly across the ankle joint. In one embodiment, a driving cap 1668 may be coupled to insertion handle 1666. In some embodiments, driving cap 1668 includes a distal end surface to which a force may be applied to facilitate insertion of nail 18. Once nail 18 has been inserted, in one embodiment, nail 18 is rotated into its final position using the driving cap 1668 and insertion handle 1666. In one embodiment, placement of nail 18 is guided and monitored using the imaging device.

Referring to FIGS. 17-20, once nail 18 is in place, in some embodiments, an aiming arm 1870 is attached to insertion handle 1666. The aiming arm 1870 may be used to insert some or all of fasteners 22 relative to the position of nail 18. In one embodiment, insertion handle 1666 includes one or more longitudinally extending alignment features 1666 a such a groove or projection. In one embodiment, alignment feature 1666 a includes a plurality of grooves spaced circumferentially around insertion handle 1666. In one embodiment, insertion handle 1666 includes a plurality of indicia 1666 b spaced radially around the insertion handle 1666. In one embodiment, indicia 1666 b are used to indicate the position of aiming arm 1870 relative to first and second longitudinal axes L₁, L₂. In one embodiment, indicia 1666 b includes markings such as letters that correspond to respective fasteners 20. For example, when aiming arm 1870 is aligned with first fastener hole 22 a, indicia 1666 b may show “C” through a viewing window in aiming arm 1870 to indicate that the hole marked “Calcaneus Screw” for calcaneus 12 should be used with the appropriate drill 1874 a, drill sleeve 1872 a and screw 20 a.

In embodiments using a compression screw, first fastener 20 a is inserted into the most distal end of first fastener hole 22 a. In such embodiments, second fastener 20 b is inserted into the most distal end of second fastener hole 22 b. For the third and fourth fasteners 20 c, 20 d, in one embodiment, there are three options 1) static locking, 2) dynamic locking and 3) originally static with the option to later make dynamic. In one embodiment, if static locking only is desired, third fastener 20 c is inserted into third fastener hole 20 c to prevent nail 18 from moving relative to tibia 16. In one embodiment, if dynamic locking only is desired, fourth fastener 20 d is inserted into the most proximal end of fourth fastener hole 22 d. In one embodiment, if it is desired to have nail 18 be static but keep the option to later make dynamic, fourth fastener 20 d is inserted into the most proximal end of fourth fastener hole 22 d and third fastener 20 c is inserted into third fastener hole 20 c. Such an embodiment prevents nail 18 from moving relative to tibia 18 until third fastener 20 c is removed at which point nail 18 may move proximally up tibia 16 if calcaneus 12 and/or talus 14 are compressed further toward tibia 16 (e.g., if bone graft compresses).

Referring to FIG. 21, once ankle fusion device 10 has been implanted, in embodiments having a compression configuration, compression screw 324 may be driven proximally through bore 18 e using a screw driver 326. In one embodiment, as compression screw 324 is driven proximally, compression screw 324 engages first fastener 22 a. Since calcaneus 12 is fixed relative to first fastener 22 a and nail 18 is prevented from moving distal due third and/or fourth fasteners 22 c, 22 d, the calcaneus is shifted proximally toward tibia 16. In one embodiment, once calcaneus 12 engages talus 14, in embodiments with an elongated second fastener hole 22 b, both calcaneus 12 and talus 14 are shifted proximally toward tibia 16.

Referring to FIG. 22, once compression screw 324 is adjusted, in one embodiment, end cap sleeve 430 and end cap screw 428 may be inserted into distal end 18 d of nail 18 to seal bore 183.

FIGS. 23A-23D illustrate an exemplary ankle fusion device 10 after installation. In one embodiment, ankle fusion device 10 is left implanted in the patient until calcaneus 12, talus 14 and/or tibia 16 are sufficiently fused together.

Referring to FIG. 24, in one embodiment, once fusion is complete or it is otherwise desired to remove ankle fusion device 10, an extraction tool 2576 may be used to assist in distracting nail 18 from the patient. In one embodiment, after removing fasteners 20 and end cap sleeve 430 and end cap screw 428, extraction tool 2576 is threadably attached to distal end 18 d of nail 18. In one embodiment, extraction tool 2576 is pulled and/or hammered distally to remove nail 18.

In one embodiment, there is a kit for performing the ankle arthrodeses described herein. Such a kit may include one or more of each of the instruments, fasteners and/or implantable devices described herein. In one embodiment, a kit for performing ankle arthrodesis includes nail 18, one or more fasteners 20, guidewire targeting device 534, and at least one guidewire 1060. In one embodiment, a kit for performing ankle arthrodesis includes nail 18, one or more fasteners 20, guidewire targeting device 534, first guidewire 1060 and second guidewire 1062. In one embodiment, a kit for performing ankle arthrodesis includes guidewire targeting device 534, and at least one guidewire 1060. In one embodiment, a kit for performing ankle arthrodesis includes guidewire targeting device 534, at least one guidewire 1060, and aiming arm 1870.

It will be appreciated by those skilled in the art that changes could be made to the exemplary embodiments shown and described above without departing from the broad inventive concept thereof. It is understood, therefore, that this invention is not limited to the exemplary embodiments shown and described, but it is intended to cover modifications within the spirit and scope of the present invention as defined by the claims. For example, specific features of the exemplary embodiments may or may not be part of the claimed invention and features of the disclosed embodiments may be combined. Unless specifically set forth herein, the terms “a”, “an” and “the” are not limited to one element but instead should be read as meaning “at least one”.

It is to be understood that at least some of the figures and descriptions of the invention have been simplified to focus on elements that are relevant for a clear understanding of the invention, while eliminating, for purposes of clarity, other elements that those of ordinary skill in the art will appreciate may also comprise a portion of the invention. However, because such elements are well known in the art, and because they do not necessarily facilitate a better understanding of the invention, a description of such elements is not provided herein.

Further, to the extent that the method does not rely on the particular order of steps set forth herein, the particular order of the steps should not be construed as limitation on the claims. The claims directed to the method of the present invention should not be limited to the performance of their steps in the order written, and one skilled in the art can readily appreciate that the steps may be varied and still remain within the spirit and scope of the present invention. 

We claim:
 1. A device for positioning at least one guidewire in a calcaneus bone and talus bone comprising: a frame configured and dimensioned to at least partially surround the calcaneus bone and the talus bone, the frame including: a guidewire target configured and dimensioned to be inserted between the talus bone and a tibia bone proximate a talar dome of the talus bone; a first guidewire sleeve radially disposed about a first guidewire axis, the first guidewire axis being aligned with the guidewire target; and a second guidewire template attached to the frame and having an alignment guide extending therefrom and a second guidewire sleeve radially disposed about a second guidewire axis, the second guidewire axis positioned at an oblique angle relative to the first guidewire axis when the alignment guide is substantially aligned with a pre-selected anatomical feature.
 2. The device of claim 1, wherein the second guidewire template is configured to rotate about the first guidewire axis.
 3. The device of claim 1, wherein the second guidewire template is slideable and rotatable relative to the first guidewire sleeve.
 4. The device of claim 1, further comprising a tibial alignment guide engaged with the frame and configured to extend proximally therefrom along a longitudinal axis substantially parallel to the first guidewire axis.
 5. The device of claim 1, wherein the frame further comprises a targeting arm that includes the guidewire target and a first sleeve arm that includes the first guidewire sleeve, the targeting arm and the first sleeve arm being substantially parallel to one another.
 6. The device of claim 1, wherein the first guidewire sleeve is fixed in position relative to the guidewire target.
 7. The device of claim 1, wherein the first guidewire axis is configured to substantially align with a center of the talar dome and to the guidewire target when the guidewire target is inserted between the talus and the tibia proximate the talar dome.
 8. The device of claim 1, wherein the first sleeve arm is positioned distally from the calcaneus bone when the guidewire target is inserted between the talus bone and the tibia bone proximate the talar dome of the talus bone.
 9. A device for positioning at least one guidewire in a calcaneus bone and talus bone comprising: a frame configured and dimensioned to at least partially surround the calcaneus bone and the talus bone, the frame including: a guidewire target configured and dimensioned to be inserted between the talus bone and a tibia bone proximate a talar dome of the talus bone; a first guidewire sleeve radially disposed about a first guidewire axis, the first guidewire axis being aligned with the guidewire target; and a second guidewire template attached to the frame and having an alignment guide extending therefrom and a second guidewire sleeve radially disposed about a second guidewire axis, the second guidewire axis extends towards the guidewire target when the alignment guide is substantially aligned with a second metatarsal bone.
 10. A device for positioning at least one guidewire in a calcaneus bone and talus bone comprising: a frame configured and dimensioned to at least partially surround the calcaneus bone and the talus bone, the frame including: a guidewire target configured and dimensioned to be inserted between the talus bone and a tibia bone proximate a talar dome of the talus bone; a first guidewire sleeve radially disposed about a first guidewire axis, the first guidewire axis being aligned with the guidewire target; and a tibial alignment guide including an extension having at least one alignment member, the tibial alignment guide engaged with the frame and configured to extend proximally therefrom along a longitudinal axis substantially parallel to the first guidewire axis, wherein the at least one alignment member is configured and positioned to intersect with a plane aligned with the first guidewire axis.
 11. The device of claim 10, wherein the first guidewire sleeve is adapted to be positioned under the calcaneus bone but not contacting the calcaneus bone.
 12. A device for positioning at least one guidewire in a calcaneus bone and talus bone comprising: a frame configured and dimensioned to at least partially surround the calcaneus bone and the talus bone, the frame including: a guidewire target configured and dimensioned to be inserted between the talus bone and a tibia bone proximate a talar dome of the talus bone; a first guidewire sleeve radially disposed about a first guidewire axis, the first guidewire axis being aligned with the guidewire target; and a tibial alignment guide rotatably attachable with the frame and configured to extend proximally therefrom along a longitudinal axis substantially parallel to the first guidewire axis.
 13. The device of claim 12, further comprising a second guidewire template attached to the frame and having a second guidewire sleeve radially disposed about a second guidewire axis.
 14. The device of claim 13, wherein the second guidewire template includes an alignment guide extending therefrom.
 15. The device of claim 14, wherein the second guidewire axis extends towards the guidewire target when the alignment guide is substantially aligned with a pre-selected anatomical feature.
 16. The device of claim 12, wherein the tibial alignment guide includes a transverse member being positionable at a location along a longitudinal axis of the tibial alignment guide.
 17. The device of claim 16, wherein the transverse member has a curvature about the first guidewire axis.
 18. The device of claim 12, wherein the frame further comprises a targeting arm that includes the guidewire target and the tibial alignment guide is attachable to the targeting arm.
 19. The device of claim 12, wherein the first guidewire sleeve is adapted to be positioned under the calcaneus bone but not contacting the calcaneus bone. 